ACAIA CORP.

FDA Device Registration & Listing · Alhambra, CA, US · Registration 3020614056

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3020614056
FEI Number
3020614056
Entity Name
ACAIA CORP.
City/State/Country
Alhambra, CA, US
Establishment Address
560 W Main Street, C808, Alhambra, CA 91801, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Acaia Corp. (Owner Number: 10087471)
Owner / Operator Contact Address
560 W Main Street, C808, Alhambra, CA 91801, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Acaia Corp

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRL Scale, Sponge, Surgical, Electrically-Powered General Hospital Class 1 880.2740 2026-03-15

Official Correspondent

Chris Cheng

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Acaia Corp.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020614056. Last updated year: 2026. Please use registration number 3020614056 when referencing this establishment in official correspondence.
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